Right aortic arch detected in fetal life

Berg, Christoph; Bender, F.; Soukup, Martin; Geipel, A.; Axt-Fliedner, R; Breuer, Judith; Herberg, Ulrike; Gembruch, Ulrich

doi:10.1002/uog.3883

Cited by 94 publications

(114 citation statements)

References 32 publications

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“…The frequency of RAA among adults is approximately 0.1%, and a similar incidence was reported in a prenatal low-risk cohort (2,3). Many undiagnosed cases are detected when RAA is investigated retrospectively.…”

Section: Discussionsupporting

confidence: 53%

“…Furthermore, RAA was associated with an extracardiac anomaly in three fetuses (25%). In a study by Berg et al,(3) this finding was observed in 12% of the entire series. These findings suggest that a meticulous inspection of fetal cardiac and extracardiac anatomy, including the brachiocephalic branching pattern, should be performed in prenatally detected cases and that cytogenetic testing for 22q11 deletions should be considered carefully.…”

Section: Discussionmentioning

confidence: 80%

See 1 more Smart Citation

Perinatal outcomes and anomalies associated with fetal right aortic arch

Gül¹,

Güngördük²,

Yıldırım³

2012

J Turkish German Gynecol Assoc

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Objective:To evaluate the prenatal findings, associated anomalies, and prognosis of right aortic arch (RAA) anomalies. Material and Methods:All cases referred for detailed ultrasonography and fetal echocardiography between October 2006 and July 2009 were systematically examined for aortic arch anomalies and associated cardiac and extracardiac anomalies. Prenatal findings of all cases with aortic arch anomalies and intracardiac and extracardiac findings were prospectively registered in an electronic database that included fetal echocardiography. Outcomes of the cases were collected postnatally from the patients' obstetricians, neonatal unit archieves, and pediatric cardiologists. Results:We detected 12 cases of RAA (0.37%; n=12/3200). Mean gestational age at diagnosis was 24 weeks (range, 21-33 weeks). Of the 12 cases of RAA, five (41.7%) had a major cardiac defect, including tetralogy of Fallot (n= 3), atrioventricular septal defect (n=1), and ventricular septal defect (n=1). An extracardiac anomaly was observed in three cases (25%). The fetal karyotype was trisomy 21 in one case with increased nuchal translucency (6.6 mm). Microdeletion 22q11 analyses performed in three cases were normal. The postnatal courses of the cases with isolated RAA were uneventful. Two cases associated with major cardiac and extracardiac anomalies were lost in the early neonatal period. The case of trisomy 21 was terminated. The other four cases of RAA with an associated cardiac anomaly are currently in follow up. Conclusion:Aortic arch anomalies, particularly RAA, can be diagnosed by fetal echocardiography. The prognosis for isolated RAA is relatively good compared with that for RAA with associated anomalies. (J Turkish-German Gynecol Assoc 2012; 13: 184-6) Key words: Right aortic arch, aortic arch anomaly, fetal echocardiography, fetus, prenatal diagnosis Received: 19 March, 2012 Accepted: 01 June, 2012 Amaç: Prenatal dönemde, sağ aortik ark tanısı alan hastaların prognozu ve diğer anomalilerle birlikteliğini değerlendirmek. Gereç ve Abstract ÖzetOriginal Investigation 184

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Section: Discussionsupporting

confidence: 53%

Section: Discussionmentioning

confidence: 80%

Perinatal outcomes and anomalies associated with fetal right aortic arch

Gül¹,

Güngördük²,

Yıldırım³

2012

J Turkish German Gynecol Assoc

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“…Another two had mild symptoms, which improved. Computed tomographic angiography and barium swallow at 2 and 5 years of age showed no significant obstruction Galindo (2009) 11 Turan (2009) 12 Hsu (2011) 32 Li (2011) 31 Bronshtein (2011) 30 Gul (2012) 29 Miranda (2014) 28 Razon (2014) 24 Chaoui (2002) 25 Achiron (2002) 2 Patel (2006) 10 Berg (2006) 8 Zidere (2006) 7 Tuo (2009) 9 Galindo (2009) 11 Turan (2009) 12 Hsu (2011) 32 Bronshtein (2011) 30 Gul (2012) 29 Miranda (2014) 28 Razon (2014) 24 Current study Galindo (2009) 11 Turan (2009) 12 Hsu (2011) 32 Li (2011) 31 Bronshtein (2011) 30 Bronshtein (1998) 6 Gul (2012) 29 Miranda (2014) 28 Achiron (2002) 2 Patel (2006) 10 Berg (2006) 8 Zidere (2006) 7 Tuo (2009) 9 Galindo (2009) 11 Turan (2009) 12 Hsu (2011) 32 Li (2011) 31 Bronshtein (2011) 30 Chaoui (2002) 25 Gul (2012) …”

Section: Cohort Studymentioning

confidence: 99%

Fetuses with right aortic arch: a multicenter cohort study and meta‐analysis

D’Antonio

Khalil

Zidere

et al. 2016

Ultrasound in Obstet & Gyne

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“…If the descending aorta lies to the right of the spinal column in levocardia, there is a right aortic arch, which is not only an isolated occurrence but also present in up to 35 % of fetuses with tetralogy of Fallot, pulmonary atresia with ventricular septum defect, and common arterial trunk (• " Fig. 13c) [29]. mit weiteren komplexen kardialen Vitien vor [14,27,28].…”

Section: Vessels Behind the Heartmentioning

confidence: 99%

“…Verläuft bei Laevokardie die deszendierende Aorta rechts der Wirbelsäule, liegt ein rechter Aortenbogen vor, der isoliert vorkommt, aber auch in bis zu 35 % der Feten mit Fallot'scher Tetralogie, Pulmonalatresie mit Ventrikelseptum-Defekt und Truncus arteriosus communis vorliegt (• " Abb. 13c) [29].…”

Section: Gefäße Hinter Dem Herzenunclassified